DK3180331T3 - POLYMORPHS OF SELINEXOR - Google Patents
POLYMORPHS OF SELINEXOR Download PDFInfo
- Publication number
- DK3180331T3 DK3180331T3 DK15754099.8T DK15754099T DK3180331T3 DK 3180331 T3 DK3180331 T3 DK 3180331T3 DK 15754099 T DK15754099 T DK 15754099T DK 3180331 T3 DK3180331 T3 DK 3180331T3
- Authority
- DK
- Denmark
- Prior art keywords
- selinexor
- polymorphs
- Prior art date
Links
- DEVSOMFAQLZNKR-RJRFIUFISA-N (z)-3-[3-[3,5-bis(trifluoromethyl)phenyl]-1,2,4-triazol-1-yl]-n'-pyrazin-2-ylprop-2-enehydrazide Chemical compound FC(F)(F)C1=CC(C(F)(F)F)=CC(C2=NN(\C=C/C(=O)NNC=3N=CC=NC=3)C=N2)=C1 DEVSOMFAQLZNKR-RJRFIUFISA-N 0.000 title 1
- 229950010613 selinexor Drugs 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4196—1,2,4-Triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462038069P | 2014-08-15 | 2014-08-15 | |
| PCT/US2015/045395 WO2016025904A1 (en) | 2014-08-15 | 2015-08-14 | Polymorphs of selinexor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DK3180331T3 true DK3180331T3 (en) | 2022-09-12 |
Family
ID=53969460
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK15754099.8T DK3180331T3 (en) | 2014-08-15 | 2015-08-14 | POLYMORPHS OF SELINEXOR |
Country Status (18)
| Country | Link |
|---|---|
| US (6) | US10519139B2 (en) |
| EP (2) | EP3180331B1 (en) |
| JP (3) | JP6777626B2 (en) |
| KR (1) | KR102608259B1 (en) |
| CN (3) | CN111484483B (en) |
| AU (4) | AU2015301484B2 (en) |
| CA (1) | CA2957266A1 (en) |
| CO (1) | CO2017001884A2 (en) |
| DK (1) | DK3180331T3 (en) |
| EA (1) | EA201790384A1 (en) |
| ES (1) | ES2926377T3 (en) |
| IL (1) | IL250328B (en) |
| MA (1) | MA40254B1 (en) |
| MX (2) | MX388170B (en) |
| SG (2) | SG10201808624VA (en) |
| UA (1) | UA123535C2 (en) |
| WO (1) | WO2016025904A1 (en) |
| ZA (1) | ZA201700880B (en) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA115532C2 (en) | 2011-07-29 | 2017-11-27 | Каріофарм Терапеутікс, Інк. | Hydrazide containing nuclear transport modulators and uses thereof |
| RS60424B1 (en) | 2012-05-09 | 2020-07-31 | Biogen Ma Inc | Nuclear transport modulators and uses thereof |
| EP2968278B8 (en) | 2013-03-15 | 2019-05-22 | Karyopharm Therapeutics Inc. | Methods of promoting wound healing using crm1 inhibitors |
| CN110183422B (en) | 2013-06-21 | 2023-07-14 | 卡尔约药物治疗公司 | Nuclear transport modulators and uses thereof |
| CN111484483B (en) * | 2014-08-15 | 2023-05-26 | 卡尔约药物治疗公司 | Polymorphs of Xilinx |
| WO2017117529A1 (en) | 2015-12-31 | 2017-07-06 | Karyopharm Therapeutics Inc. | Nuclear transport modulators and uses thereof |
| MA43530A (en) | 2015-12-31 | 2018-11-07 | Karyopharm Therapeutics Inc | NUCLEAR TRANSPORT MODULATORS AND THEIR USES |
| WO2017118940A1 (en) | 2016-01-08 | 2017-07-13 | Dr. Reddy's Laboratories Limited | Solid forms of selinexor and process for their preparation |
| WO2018098472A1 (en) | 2016-11-28 | 2018-05-31 | Karyopharm Therapeutics Inc. | Crm1 inhibitors for treating epilepsy |
| WO2018129227A1 (en) | 2017-01-05 | 2018-07-12 | Watson Laboratories Inc. | Novel crystalline forms of selinexor and process for their preparation |
| CN106831731B (en) * | 2017-01-17 | 2019-11-08 | 广州市闻皓生物科技有限公司 | A kind of synthetic method of Selinexor bulk pharmaceutical chemicals |
| WO2019232724A1 (en) | 2018-06-06 | 2019-12-12 | Xw Laboratories, Inc. | Compounds as nuclear transport modulators and uses thereof |
| WO2020072008A1 (en) * | 2018-10-04 | 2020-04-09 | Deva Holding Anonim Sirketi | Novel solid dispersions of selinexor |
| JP2022524741A (en) * | 2019-03-20 | 2022-05-10 | ジョンソン、マッセイ、パブリック、リミテッド、カンパニー | Co-crystal morphology of serinexol |
| MA55808A (en) * | 2019-05-01 | 2022-03-09 | Karyopharm Therapeutics Inc | METHOD FOR PREPARING XPO1 INHIBITORS AND INTERMEDIATES FOR USE IN PREPARING XPO1 INHIBITORS |
| EP3968987A4 (en) * | 2019-05-16 | 2022-10-26 | Mayo Foundation for Medical Education and Research | METHODS AND SUBSTANCES FOR THE TREATMENT OF CANCER |
| EP3808742A1 (en) | 2019-10-16 | 2021-04-21 | Sandoz AG | Polymorph of selinexor |
| US20230391754A1 (en) | 2020-10-21 | 2023-12-07 | Karyopharm Therapeutics Inc. | Crystalline form of selinexor |
| CN112679477B (en) * | 2020-12-17 | 2021-10-26 | 佛山奕安赛医药科技有限公司 | Preparation method of celecoxib and intermediate thereof |
| CA3243305A1 (en) * | 2021-12-20 | 2023-06-29 | Rtx Corp | Particle enhancement of ceramic matrix composites, method of manufacture thereof and articles comprising the same |
| CN116675677B (en) * | 2023-08-02 | 2023-09-26 | 中国林业科学研究院林产化学工业研究所 | C8 urushiol derivative and preparation method and application thereof |
Family Cites Families (73)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1017398A (en) | 1911-01-16 | 1912-02-13 | John E Folsom | Telegraph-key. |
| KR840000529A (en) | 1981-07-07 | 1984-02-25 | 콘스탄틴 루이스 클레멘트 | Method for preparing indole derivative |
| CS229934B2 (en) | 1981-07-07 | 1984-07-16 | Pfizer | Production method subst.indolylacryte acid derivative |
| US4778796A (en) | 1985-07-19 | 1988-10-18 | Dainippon Pharmaceutical Co., Ltd. | ω-(3-pyridyl)alkenamide derivatives and anti-allergenic pharmaceutical compositions containing same |
| IL97249A (en) | 1990-02-23 | 1995-01-24 | Takeda Chemical Industries Ltd | 4,5,6,7- Tetrahydrothiazolo (5,4-b) pyridine and 5,6-dihydro-4h pyrrolo (3,2-d) thiazolo compounds, their production and pharmaceutical compositions containing them |
| JP3111321B2 (en) | 1990-02-23 | 2000-11-20 | 武田薬品工業株式会社 | Condensed thiazole compound |
| US5541213A (en) | 1993-06-24 | 1996-07-30 | Eisai Co., Ltd. | Propenoic acid derivatives diazole propenoic acid compounds which have useful pharmaceutical utility |
| US5468353A (en) | 1994-05-05 | 1995-11-21 | Minnesota Mining And Manufacturing Company | Mist suppressant for solvent extraction metal electrowinning |
| AU4368996A (en) | 1994-11-23 | 1996-06-17 | Neurogen Corporation | Certain 4-aminomethyl-2-substituted imidazole derivatives and 2-aminomethyl-4-substituted imidazole derivatives; new classes of dopamine receptor subtype specific ligands |
| US20030018025A1 (en) | 1995-06-07 | 2003-01-23 | Neurogen Corporation, Corporation Of The State Of Delaware | Certain 4-aminomethyl-2-substituted imidazole derivatives and 2-aminomethyl-4-substituted imidazole derivatives: new classes of dopamine receptor subtype specific ligands |
| EP0858457A1 (en) | 1995-10-20 | 1998-08-19 | Dr. Karl Thomae GmbH | 5-membered heterocycles, pharmaceutical agents containing said compounds and the use thereof and methods of producing them |
| CN1088711C (en) | 1996-04-04 | 2002-08-07 | 盐野义制药株式会社 | Cephem compound and medicine containing the compound |
| JP4054992B2 (en) | 1996-04-25 | 2008-03-05 | 日産化学工業株式会社 | Ethylene derivatives and pest control agents |
| DE69723267T2 (en) | 1996-04-25 | 2004-04-22 | Nissan Chemical Industries, Ltd. | ETHYLENE DERIVATIVES AND PESTICIDES |
| DE19624659A1 (en) | 1996-06-20 | 1998-01-08 | Klinge Co Chem Pharm Fab | New pyridylalkene and pyridylalkanoic acid amides |
| US5994398A (en) | 1996-12-11 | 1999-11-30 | Elan Pharmaceuticals, Inc. | Arylsulfonamides as phospholipase A2 inhibitors |
| JP4416198B2 (en) | 1997-12-19 | 2010-02-17 | 武田薬品工業株式会社 | Anilide derivatives, their production and use |
| AU2960599A (en) | 1998-03-30 | 1999-10-18 | Akira Karasawa | Quinazoline derivatives |
| US6743585B2 (en) | 1999-09-16 | 2004-06-01 | Agilent Technologies, Inc. | Methods for preparing conjugates |
| CO5271680A1 (en) | 2000-02-21 | 2003-04-30 | Smithkline Beecham Corp | COMPOUNDS |
| EP1335898B1 (en) | 2000-09-29 | 2005-11-23 | TopoTarget UK Limited | Carbamic acid compounds comprising an amide linkage as hdac inhibitors |
| EP1429765A2 (en) | 2001-09-14 | 2004-06-23 | Methylgene, Inc. | Inhibitors of histone deacetylase |
| WO2004037248A2 (en) | 2002-10-24 | 2004-05-06 | Carex Sa | Modulation of peroxisome proliferator activated receptors activity |
| DE10250743A1 (en) | 2002-10-31 | 2004-05-19 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | New amide compounds having MCH antagonist activity and medicaments containing these compounds |
| JP4145230B2 (en) | 2002-11-01 | 2008-09-03 | 武田薬品工業株式会社 | Preventive and therapeutic agents for neurological disorders |
| BR0315815A (en) | 2002-11-01 | 2005-09-13 | Takeda Pharmaceutical | Agents for preventing or treating neuropathy, for promoting the production or secretion of a neurotropic factor, for improving pain, neuroprotective and pharmaceutical compound, methods for preventing or treating neuropathy and for promoting the production or secretion of a neurotropic factor. improve pain to protect a nerve in a mammal and produce a compound and use of a compound |
| CA2504941C (en) | 2002-11-08 | 2012-06-26 | Neurogen Corporation | 3-substituted-6-aryl pyridines |
| CA2512886A1 (en) | 2003-02-28 | 2004-09-10 | Galderma Research & Development, S.N.C. | Ligands that modulate lxr-type receptors |
| MY149038A (en) | 2004-05-26 | 2013-07-15 | Eisai R&D Man Co Ltd | Cinnamide compound |
| KR20070050475A (en) | 2004-08-11 | 2007-05-15 | 교린 세이야꾸 가부시키 가이샤 | New Cyclic Amino Benzoate Derivatives |
| WO2006019020A1 (en) | 2004-08-16 | 2006-02-23 | Sankyo Company, Limited | Substituted ureas |
| EP1849465A4 (en) | 2005-02-18 | 2008-12-24 | Takeda Pharmaceutical | AGENT FOR CONTROLLING THE FUNCTION OF THE GPR34 RECEPTOR |
| WO2007058338A2 (en) | 2005-11-15 | 2007-05-24 | Otsuka Pharmaceutical Co., Ltd. | Oxazole compound and pharmaceutical composition |
| JP2007210929A (en) | 2006-02-09 | 2007-08-23 | Sankyo Co Ltd | Medicine containing urea compound |
| EP1992618B1 (en) | 2006-03-09 | 2012-01-18 | Eisai R&D Management Co., Ltd. | Polycyclic cinnamide derivative |
| ES2452820T3 (en) | 2006-04-07 | 2014-04-02 | Methylgene, Inc. | Benzamide derivatives as histone deacetylase inhibitors |
| NZ572268A (en) | 2006-04-18 | 2011-09-30 | Nippon Chemiphar Co | Activating agent for peroxisome proliferator activated receptor delta (ppar) |
| EP2030974B1 (en) | 2006-06-13 | 2016-02-17 | Shanghai Institute of Materia Medica, Chinese Academy of Sciences | Thiazole non-nucleoside compounds, their preparation, pharmaceutical composition and their use as antiviral agents |
| EP2054411B1 (en) | 2006-07-27 | 2014-08-20 | Amorepacific Corporation | Novel compounds, isomer thereof, or pharmaceutically acceptable salts thereof as vanilloid receptor antagonist; and pharmaceutical compositions containing the same |
| US8273738B2 (en) | 2006-09-05 | 2012-09-25 | Kyowa Hakko Kirin Co., Ltd. | Imidazole derivatives |
| EP1942104A1 (en) | 2006-12-20 | 2008-07-09 | sanofi-aventis | Heteroarylcyclopropanecarboxamides and their use as pharmaceuticals |
| EP1939180A1 (en) | 2006-12-20 | 2008-07-02 | sanofi-aventis | Heteroarylacrylamides and their use as pharmaceuticals for the stimulation of the expression of endothelial NO synthase |
| CN101711154A (en) | 2007-02-26 | 2010-05-19 | 科森生物科学公司 | carbamate compound |
| EP2003118A1 (en) | 2007-06-13 | 2008-12-17 | Bayer Schering Pharma Aktiengesellschaft | Cinnamic acid derivatives as modulators of EP2 receptors |
| EP2323737A2 (en) | 2008-08-08 | 2011-05-25 | Synta Pharmaceuticals Corp. | Triazole compounds that modulate hsp90 activity |
| JP2012532889A (en) | 2009-07-09 | 2012-12-20 | クレッシェンド セラピューティクス、エルエルシー | Wound treatment method and scar degeneration method |
| WO2011069039A1 (en) | 2009-12-04 | 2011-06-09 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Hydrazone and diacyl hydrazine compounds and methods of use |
| AU2011222531B2 (en) | 2010-03-05 | 2015-03-26 | Karyopharm Therapeutics, Inc. | Nuclear transport modulatiors and uses thereof |
| EP2665362B1 (en) | 2011-01-17 | 2016-03-30 | Karyopharm Therapeutics, Inc. | Olefin containing nuclear transport modulators and uses thereof |
| UA115532C2 (en) * | 2011-07-29 | 2017-11-27 | Каріофарм Терапеутікс, Інк. | Hydrazide containing nuclear transport modulators and uses thereof |
| MX350442B (en) | 2011-07-29 | 2017-09-06 | Karyopharm Therapeutics Inc | Nuclear transport modulators and uses thereof. |
| WO2013020024A2 (en) | 2011-08-03 | 2013-02-07 | Karyopharm Therapeutics, Inc. | Maleimide compounds and methods of treatment |
| RS60424B1 (en) | 2012-05-09 | 2020-07-31 | Biogen Ma Inc | Nuclear transport modulators and uses thereof |
| EP2968278B8 (en) * | 2013-03-15 | 2019-05-22 | Karyopharm Therapeutics Inc. | Methods of promoting wound healing using crm1 inhibitors |
| US20160016916A1 (en) | 2013-03-15 | 2016-01-21 | Karyopharm Therapeutics Inc. | Exo Olefin-Containing Nuclear Transport Modulators and Uses Thereof |
| WO2014205393A1 (en) | 2013-06-21 | 2014-12-24 | Karyopharm Therapeutics Inc. | Nuclear transport modulators and uses thereof |
| CN110183422B (en) | 2013-06-21 | 2023-07-14 | 卡尔约药物治疗公司 | Nuclear transport modulators and uses thereof |
| US11567063B2 (en) * | 2013-11-15 | 2023-01-31 | H. Lee Moffitt Cancer Center And Research Institute, Inc. | Methods for assessing cell viability or predicting cell response to a treatment using cell movement |
| US10969391B2 (en) | 2014-07-11 | 2021-04-06 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for diagnosing hematological cancers |
| WO2016015597A1 (en) * | 2014-07-26 | 2016-02-04 | Sunshine Lake Pharma Co., Ltd. | Compounds as cdk small-molecule inhibitors and uses thereof |
| CN111484483B (en) | 2014-08-15 | 2023-05-26 | 卡尔约药物治疗公司 | Polymorphs of Xilinx |
| WO2017040311A1 (en) | 2015-08-28 | 2017-03-09 | The Trustees Of Columbia University In The City Of New York | Systems and methods for matching oncology signatures |
| MA43530A (en) | 2015-12-31 | 2018-11-07 | Karyopharm Therapeutics Inc | NUCLEAR TRANSPORT MODULATORS AND THEIR USES |
| WO2017117529A1 (en) | 2015-12-31 | 2017-07-06 | Karyopharm Therapeutics Inc. | Nuclear transport modulators and uses thereof |
| WO2017118940A1 (en) | 2016-01-08 | 2017-07-13 | Dr. Reddy's Laboratories Limited | Solid forms of selinexor and process for their preparation |
| JP6765198B2 (en) | 2016-03-10 | 2020-10-07 | パナソニック株式会社 | Latent heat storage material and heat storage system using it |
| WO2018098472A1 (en) | 2016-11-28 | 2018-05-31 | Karyopharm Therapeutics Inc. | Crm1 inhibitors for treating epilepsy |
| WO2018129227A1 (en) * | 2017-01-05 | 2018-07-12 | Watson Laboratories Inc. | Novel crystalline forms of selinexor and process for their preparation |
| CN106831731B (en) | 2017-01-17 | 2019-11-08 | 广州市闻皓生物科技有限公司 | A kind of synthetic method of Selinexor bulk pharmaceutical chemicals |
| CA3131720A1 (en) | 2019-03-27 | 2020-10-01 | Andrea Califano | Biomarkers for selinexor |
| EP3808742A1 (en) | 2019-10-16 | 2021-04-21 | Sandoz AG | Polymorph of selinexor |
| US11828455B2 (en) | 2019-12-06 | 2023-11-28 | Bae Systems Plc | Light source |
| US20230391754A1 (en) | 2020-10-21 | 2023-12-07 | Karyopharm Therapeutics Inc. | Crystalline form of selinexor |
-
2015
- 2015-08-14 CN CN202010093491.4A patent/CN111484483B/en active Active
- 2015-08-14 EA EA201790384A patent/EA201790384A1/en unknown
- 2015-08-14 MA MA40254A patent/MA40254B1/en unknown
- 2015-08-14 AU AU2015301484A patent/AU2015301484B2/en active Active
- 2015-08-14 SG SG10201808624VA patent/SG10201808624VA/en unknown
- 2015-08-14 JP JP2017508087A patent/JP6777626B2/en active Active
- 2015-08-14 CN CN202010093239.3A patent/CN111481553B/en active Active
- 2015-08-14 UA UAA201702169A patent/UA123535C2/en unknown
- 2015-08-14 CN CN201580056017.1A patent/CN107072992B/en active Active
- 2015-08-14 MX MX2017002013A patent/MX388170B/en unknown
- 2015-08-14 DK DK15754099.8T patent/DK3180331T3/en active
- 2015-08-14 CA CA2957266A patent/CA2957266A1/en active Pending
- 2015-08-14 US US15/503,319 patent/US10519139B2/en active Active
- 2015-08-14 EP EP15754099.8A patent/EP3180331B1/en active Active
- 2015-08-14 ES ES15754099T patent/ES2926377T3/en active Active
- 2015-08-14 WO PCT/US2015/045395 patent/WO2016025904A1/en not_active Ceased
- 2015-08-14 EP EP22176543.1A patent/EP4112615A1/en active Pending
- 2015-08-14 SG SG11201700789SA patent/SG11201700789SA/en unknown
- 2015-08-14 KR KR1020177006680A patent/KR102608259B1/en active Active
-
2017
- 2017-01-29 IL IL250328A patent/IL250328B/en unknown
- 2017-02-03 ZA ZA2017/00880A patent/ZA201700880B/en unknown
- 2017-02-14 MX MX2021014128A patent/MX2021014128A/en unknown
- 2017-02-24 CO CONC2017/0001884A patent/CO2017001884A2/en unknown
-
2019
- 2019-11-11 US US16/679,630 patent/US11078190B2/en active Active
-
2020
- 2020-05-19 AU AU2020203246A patent/AU2020203246B2/en active Active
- 2020-05-29 JP JP2020093874A patent/JP7218323B2/en active Active
-
2021
- 2021-07-01 US US17/365,656 patent/US11807629B2/en active Active
- 2021-12-14 AU AU2021286266A patent/AU2021286266B2/en active Active
-
2023
- 2023-01-25 JP JP2023009361A patent/JP7558310B2/en active Active
- 2023-04-05 US US18/131,273 patent/US11753401B2/en active Active
- 2023-04-07 US US18/132,241 patent/US11746102B2/en active Active
- 2023-07-26 US US18/226,570 patent/US12371420B2/en active Active
-
2024
- 2024-04-30 AU AU2024202835A patent/AU2024202835A1/en active Pending
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DK3180331T3 (en) | POLYMORPHS OF SELINEXOR | |
| DK3137169T3 (en) | INHIBITORIES OF LYSIN-SPECIFIC DEMETHYLASE-1 | |
| DK3134530T3 (en) | TREATMENT OF HYPERBILIR RUBINY | |
| DK3102576T3 (en) | DIHYDROPYRROLOPYRIDINE INHIBITORS OF ROR-GAMMA | |
| DK3192902T3 (en) | PROCEDURE FOR THE MANUFACTURE OF GRAPHENCY VISCOSEFIBREES | |
| DK3201410T3 (en) | IMPROVEMENTS OF BUILDING COVERINGS | |
| DK3164380T3 (en) | INHIBITORS OF LIGHT-SPECIFIC DEMETHYLASE-1 | |
| DK3514109T3 (en) | HYDROPYROLYSE OF BIOMASSIC RAW MATERIALS | |
| DK3117030T3 (en) | DIAGNOSIS OF SEPSIS | |
| DK3558961T3 (en) | Polymorphs | |
| DK3558995T3 (en) | Polymorphs | |
| DK3233813T3 (en) | PROCEDURES FOR THE PREPARATION OF OXATHIAZINE-LIKE COMPOUNDS | |
| DK3132009T3 (en) | COURSE OF ACTION | |
| DK3220891T3 (en) | SUBLINGUAL FORMULATION OF RILUZOL | |
| DK3283210T3 (en) | COURSE OF ACTION | |
| DK3204352T3 (en) | Inhibitors of lysine-gingipain | |
| DK3418273T3 (en) | Derivatives of flavaglines | |
| DK3511000T3 (en) | CRYSTALLINIC FORM X2 OF GRAPIPRANT | |
| DK3297619T3 (en) | Therapeutic uses of L-4-chlorokynurenine | |
| DK3368044T3 (en) | TREATMENT OF HEPATIC STEATOSE-RELATED OLIGO-OVULATION | |
| DK3201323T3 (en) | Modification of bacteriophage | |
| IL254502A0 (en) | Solid forms of menaquinols | |
| DK3137449T3 (en) | METHODS OF PREPARING SUBSTITUTED CYCLOSERINES | |
| DK2910535T3 (en) | COMPOSITION FOR USE OF EXPANDED PERLIT | |
| DK3430004T3 (en) | SOLID FORMS OF NILOTINE INSALTS |